Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome

Microduplication of 15q13.3 and Xq21.31 in a family with tourette syndrome and comorbidities

(2013) Linea Melchior et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

DISC1in adult ADHD patients: An association study in two European samples

(2013) Kaya K. Jacobsen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Dysfunction ofSHANK2andCHRNA7in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci

(2013) B Chilian et al.   CLINICAL GENETICS

The genetic basis of Gilles de la Tourette Syndrome

(2013) Peristera Paschou   NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS

Prioritization of Copy Number Variation Loci Associated with Autism from AutDB–An Integrative Multi-Study Genetic Database

(2013) Idan Menashe et al.   PLoS One

The Gilles De La Tourette syndrome: the current status

(2012) Mary May Robertson   Archives of Disease in Childhood-Education and Practice Edition

Good Response to Clonidine in Tourette Syndrome Associated With Chromosomal Translocation Involving the IMMP2L Gene

(2012) Isurima Katuwawela et al.   JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES

ER Stress, Mitochondrial Dysfunction and Calpain/JNK Activation are Involved in Oligodendrocyte Precursor Cell Death by Unconjugated Bilirubin

(2012) Andreia Barateiro et al.   NEUROMOLECULAR MEDICINE

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

(2012) Claire S. Leblond et al.   PLoS Genetics

Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism

(2012) R A Clarke et al.   Translational Psychiatry

Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3

(2011) Nigel M. Williams et al.   AMERICAN JOURNAL OF PSYCHIATRY

Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome

(2011) Chirag Patel et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Deficiency in the inner mitochondrial membrane peptidase 2-like (Immp21) gene increases ischemic brain damage and impairs mitochondrial function

(2011) Yi Ma et al.   NEUROBIOLOGY OF DISEASE

Exon expression and alternatively spliced genes in tourette syndrome

(2010) Yingfang Tian et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Cerebellar morphology in Tourette syndrome and obsessive-compulsive disorder

(2009) Russell H. Tobe et al.   ANNALS OF NEUROLOGY

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

(2009) B W M van Bon et al.   JOURNAL OF MEDICAL GENETICS

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

(2009) J Elia et al.   MOLECULAR PSYCHIATRY

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility

(2009) E Maestrini et al.   MOLECULAR PSYCHIATRY

Validation of the Presence of Comorbidities in a Danish Clinical Cohort of Children With Tourette Syndrome

(2008) Nanette M. M. Mol Debes et al.   JOURNAL OF CHILD NEUROLOGY

Mitochondrial Dysfunction and Psychiatric Disorders

(2008) Gislaine T. Rezin et al.   NEUROCHEMICAL RESEARCH

Mitochondria in Neuroplasticity and Neurological Disorders

(2008) Mark P. Mattson et al.   NEURON

A Mutation in the Inner Mitochondrial Membrane Peptidase 2-Like Gene (Immp2l) Affects Mitochondrial Function and Impairs Fertility in Mice1

(2007) Baisong Lu et al.   BIOLOGY OF REPRODUCTION